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Differential
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abducens nerve paralysis

adenosine deaminase deficiency

adverse drug reaction

agenesis of corpus callosum

alcohol, neurologic complications with

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

anterior spinal artery

apnea, primary central

apraxia of eye movements

Arnold Chiari malformation

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

atlanto-axial subluxation

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

bone marrow biopsy

brainstem, atrophy

brainstem, dysfunction

brainstem, hypoplasia

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

Brown-Vialetto-Van Laere syndrome

Canavan's disease

carotid angiogram

CAT scan, abnormal

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar peduncle

cerebellar vermis

cerebellum, disease of

cerebellum, neoplasms of

cerebrospinal fluid

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Chediak-Higashi syndrome

cherry red spot

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

complicated migraine

congenital malformation

congenital ocular motor apraxia

contractures, joint

conus medullaris, lesion of

corneal dystrophy

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

cultured skin fibroblasts

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

degenerative diseases of CNS

dementia, familial

dementia, frontotemporal

dementia, presenile

demyelinating disease

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetes mellitus, ocular complications in

diabetic cranialneuropathies

diagnostic criteria

differential diagnosis

disconnection syndrome

down-beat nystagmus

down-beat nystagmus, primary position of gaze

dysdiadochokinesia

electroencephalogram

electroencephalogram, abnormalities of

electronystagmography

electroretinograph

epidemiology of neurology

episodic disorders

episodic neurologic deficits

evoked potentials

eye movement, disorders of

Fabry's disease

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

feeding disorder

finger nose finger test

fourth ventricle, enlargement of

Friedreich's ataxia

frontotemporal dementia, behavioral variant

fundus, abnormality of

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

granulomatosis with polyangiitis

granulomatous disease

head circumference

hemangioblastoma

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatosplenomegaly

Horner's syndrome

hyperthyroidism

hypertriglyceridemia

hypofibrinogenemia

hypomyelination

immunologic disease

immunosuppression

inborn errors of metabolism

inclusion bodies, intracytopasmic

infantile bilateral striatal necrosis

infection, recurrent

intellectual deficit

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intracranial pressure, increased

Jakob-Creutzfeldt disease

Joubert syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

Leber's congenital amaurosis

Leigh's disease

leukocyte peroxidase

leukoencephalopathy

leukoencephalopathy, differential diagnosis

light-near dissociation, causes of

lipid storage disorder of CNS

livedo reticularis

lymphadenopathy

lymphoma involving CNS

lymphomatoid granulomatosis

malformation, CNS, congenital

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

memory, impairment of

meningitis, carcinomatous

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

mitochondrial disease

molecular genetics

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, contrast enhanced

MRI, spinal cord

multiple sclerosis, differential diagnosis of

multiple system atrophy

myasthenia gravis

myasthenia gravis, familial incidence of

myasthenia gravis, nystagmus in

myasthenia gravis, ocular

myasthenia gravis, sensory loss with

myoclonic jerks

myoclonus, epilepsy

nausea and vomiting

neoplasm, primary of CNS

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuronopathy, sensory

neuroophthalmology

neuropathy, demyelinating

neuropathy, peripheral

next-generation sequencing

Niemann-Pick disease

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, monocular

nystagmus, pendular

nystagmus, periodic

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

ocular motility, disorders of

ophthalmic artery occlusion

ophthalmoplegia

optical coherence tomography

optokinetic nystagmus, abnormal

palatal myoclonus

paraparesis, spastic

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

Pelizaeus Merzbacher

personality change

pleocytosis of cerebrospinal fluid

pons, hypoplasia

precipitating factors

pregnancy, neurologic complications in

pretectal syndrome

primary episodic ataxia

progressive neurologic disorder

pseudointernuclear ophthalmoplegia

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyramidal tract, uncrossed

pyruvate metabolism, abnormality of

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

release phenomena

renal tubular acidosis

respiratory failure

retinal degeneration

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

riboflavin transporter deficiency

scoliosis, neurologic association with

seizure, children

sensorineural hearing loss

sensory loss, leg

skin, lesions in neurologic disorders

Sneddon's syndrome

spastic diplegia

speech, loss of

spinal cord, ischemic lesion of

spinal cord, neoplasm

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar degeneration

spinopontine atrophy, dominant

spongy degeneration of brain

status epilepticus

steroid therapy, CNS treatment and complications with

stress, emotional

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

subcortical U fibers

syphilis, neurologic complications with

tandem gait, ataxic

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

urinary incontinence

vertigo, episodic

vertigo, treatment of

vestibular areflexia

vision, failure of in childhood

visual acuity, decreased

visual evoked response

Von Hippel Lindau

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, progressive

white matter disease

wide based gait

Wolfram syndrome

Showing articles 1550 to 1600 of 2207 << Previous Next >>

Wilson's Disease Studies with FDG & Positron Emission Tomography
Neurol 37:1707-1711, Hawkins,R.A.,et al, 1987

Essential Tremor:A Review
Neurol 37:1194-1197, Findley,L.J.&Koller,W.C., 1987

A Rating Scale for Gilles de la Tourette's Syndrome:Description, Reliability, & Validity Data
Neurol 37:1542-1544, Goetz,C.G.,et al, 1987

Alzheimer's Disease
Down's Syndrome, & Chromosome 21, Editorial, Lancet 1:1011-1012., , 1987

Risk Factors for Alzheimer's Disease:A Case-Control Study
Neurol 37:1630-1633, Shalat,S.T.,et al, 1987

Multiple Sclerosis & Systemic Lupus Erythematosus, Occurrence in Two Generations of the Same Family
Arch Int Med 147:1317-1320, Sloan,J.B.,et al, 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Human T-Lymphotropic Virus Type I Antibodies in The Serum of Pts with Tropical Spastic Paraparesis in the Seychelles
Arch Neurol 44:605-607, Roman,G.C.,et al, 1987

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Magnetic Resonance Imaging in Isolated Noncompressive Spinal Cord Syndromes
Ann Neurol 22:714-723, Miller,D.H.,et al, 1987

The Aetiology of Mirror Writing:A New Hypothesis
JNNP 50:1572-1578, Tashiro,K.,et al, 1987

Alternating Hemiplegia of Childhood
Int Pediatr 2:115-119, Aicardi,J., 1987

Hereditary Neuropathy with Liability to Pressure Palsies
In Handbk of Clin Neurol, Elsevier Sci Publ Co, NY 51:551-562987., Cherry,S.&Mayer,R.F., 1987

Evidence That the Gene for Tuberous Sclerosis is on Chromosome 9
Lancet 1:659-661, Fryer,A.E.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Neurofibromatosis
Editorial, Lancet 1:663-6641987., , 1987

Renal Cell Carcinoma in von Hippel-Lindau Syndrome
Am J Med 82:236-238, Malek,R.S.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Familial Occurrence of Spontaneous Dissection of the Internal Carotid Artery
Stroke 18:246-251, Mokri,B.,et al, 1987

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

Eye-Movement Disorders in Brain-Stem & Cerebellar Stroke
Arch Neurol 44:141-148, Bogousslavsky,J.&Meienberg,O., 1987

Tourette Syndrome
Editorial, Lancet 1:3081987., , 1987

Caffeine & Tremor
Neurol 37:169-172, Koller,W.,et al, 1987

Dementia of the Alzheimer Type:Clinical & Family Study of 22 Twin Pairs
Neurol 37:359-363, Nee,L.E.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987

Tropical Spastic Paraparesis:HTLV-I Antibodies in Patients from the Seychelles
NEJM 316:51, Roman,G.C.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

Antibody to Human T-Lymphotropic Virus Type I In West-Indian-Born UK Residents with Spastic Paraparesis
Lancet 1:415-416, Newton,M.,et al, 1987

Tobacco-Induced Primary-Position Upbeat Nystagmus
Ann Neurol 21:53-58, Sibony,P.A.,et al, 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Benign Positional Vertigo:Clinical & Oculographic Features in 240 Cases
Neurol 37:371-378, Baloh,R.W.,et al, 1987

Upbeat Nystagmus:Clinicopathologic Study of Two Patients
Neurol 37:491-494, Keane,J.R.&Itabashi,H.H., 1987

False Negative Results in Patients with fra (X) (q) Mental Retardation Taking Oral Vitamin Supplements
NEJM 316:1093, Froster-Iskenius,U.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Dorsal Midbrain Syndrome in Multiple Sclerosis with Magnetic Resonance Imaging Correlation
Can J Neurol Sci 13:62-65, Costantino,A.,et al, 1986

Magnetic Resonance Imaging in Clinically Isolated Lesions of the Brain Stem
JNNP 49:737-743, Ormerod,I.E.C.,et al, 1986

Keyhole Aqueduct Syndrome
Arch Neurol 43:926-929, delaMonte,S.M.,et al, 1986

Bilateral Ocular Motor Signs After Tentorial Herniation in 25 Patients
Arch Neurol 43:806-807, Keane,J.R., 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Familial Long Thoracic Nerve Palsy:A Manifestation of Brachial Plexus Neuropathy
Neurol 36:1251-1253, Phillips,L.H., 1986

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Showing articles 1550 to 1600 of 2207 << Previous Next >>